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Data sourced from ClinicalTrials.gov. Always consult a healthcare provider before enrolling.

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CompletedPhase 2

A Study to Evaluate the Safety and Efficacy of CT1812 in Subjects With Mild to Moderate Alzheimer's Disease.

This is a multi-center, randomized, double-blind, placebo-controlled, parallel group 36 week multicenter Phase 2 study of two doses of CT1812 in adults with mild to moderate Alzheimer's Disease (AD).

Phoenix, Arizona, United States+31 moreView details
CompletedPhase 1

Augmenting Flortaucipir Dosimetry Estimates

This study will obtain data from urine in subjects administered flortaucipir in an Avid-sponsored study to augment the calculation of radiation dosimetry estimates.

New Haven, Connecticut, United StatesView details
Unknown

University of Washington Alzheimer's Disease Research Center (UW ADRC) Imaging & Biomarker Core

This is a cross-sectional, observational study that characterizes research participants with Alzheimer's disease (AD) for their patterns of brain degeneration with the investigational tau positron emission tomography (PET) radiotracer \[18F

Multiple locationsView details
RecruitingPhase 2

Combined Brain Stimulation and Methylphenidate Treatment for Apathy in Dementia

This study evaluates whether the combined treatment of methylphenidate and non-invasive brain stimulation, called intermittent theta burst stimulation, can effectively treat apathy in individuals with Alzheimer's disease or mixed AD/vascula

Toronto, Ontario, CanadaView details
Active, not recruitingPhase 2

Study of SPG302 in Adult Participants With Mild-to-Moderate Alzheimer's Disease (AD)

This phase 2 study will evaluate the safety, tolerability, clinical efficacy, pharmacokinetics, and pharmacodynamics of SPG302 in adult participants with mild-to-moderate AD.

Sydney, New South Wales, Australia+1 moreView details
CompletedN/A

Evaluation of an Innovative Information, Training and Social Support Intervention "INFOSADEM" to Principal Caregivers of Dementia Patients Living at Home

Background: Dementia is an illness that mostly affects people of advanced age and causes disability and dependency. Although the difficulties, a vast number of older people with dementia at our context, are cared for in their own homes by a

Multiple locationsView details
Terminated

Relationship Between Protein Biomarkers in Cerebrospinal Fluid and Alzheimer&Apos;s Disease in Patients With Depression

It is currently accepted that depression during midlife is a risk factor for Alzheimer's disease (AD). Furthermore, several prospective population studies have demonstrated that depression is an independent risk factor for incident dementia

Tortosa, Tarragona, SpainView details
Active, not recruitingPhase 2 / Phase 3

Piromelatine 20 mg in Participants With Mild Dementia Due to Alzheimer's Disease

Randomized efficacy and safety study of piromelatine 20 mg versus placebo in participants with mild dementia due to Alzheimer's disease (AD) who are 2:107,510,000-107,540,000 polymorphism non-carriers with the primary objective to compare t

Costa Mesa, California, United States+36 moreView details
CompletedN/A

Analysis of XTR006 PET Imaging in Non-cognitively Impaired Subjects, MCI Due toAD, and Mild to Moderate AD Subjects

This is an investigator-initiated clinical (IIT)study.The main purpose of this study was to evaluate the diagnostic efficacy of XTR006 PET qualitative reading and quantitative analysis in detecting mild cognitive impairment(MCI)due to AD an

Beijing, Beijing Municipality, ChinaView details
By invitationN/A

Software Validation Study-Cognitive Status Indicator

The SPARK Cognitive Status Indicator software uses an algorithm to assess a resting state EEG recording as being consistent with a cognitive status of unimpaired, mild cognitive impairment (MCI; MCI AD- or MCI AD+), or dementia (dementia AD

Miami, Florida, United StatesView details
CompletedPhase 1

Evaluation of Imaging Characteristics of [18F]PI-2620 PET in AD and PSP Patients Using High and Low Specific Activity

This is an open-label study without randomisation. All eligible patients will receive two administrations of the investigational imaging agent \[18F\]PI-2620 at a radioactive dose of 185 MBq, one with high specific activity (≤ 5 µg tracer m

Leipzig, GermanyView details
RecruitingN/A

Pilot Study on the Feasibility of Using Smartphone Data as a Diagnostic Marker for Alzheimer's Disease

This study will compare smartphone usage data between three groups of patients diagnosed with either a memory complaint, mild cognitive decline, or Alzheimer's disease.

Poitiers, FranceView details
Completed

Rehabilitation of Facial Emotion Recognition in Alzheimer's Disease

EYE-TAR(AD+) is an observational study based on the same design as the princeps EYE-TAR(MA) study, but with a larger number of patients and including an additional evaluation of Facial emotion recognition (based on a more ecological materia

Monaco, MonacoView details
CompletedN/A

Clinical Trial of Donepezil Between the Patients With Alzheimer's Disease and Mixed Dementia

To compare the clinical efficacy of donepezil between patients with Alzheimer's disease and Mixed Dementia.

Seoul, South KoreaView details
CompletedPhase 4

The Effectiveness And Safety Of Donepezil Hydrochloride (E2020) In Subjects With Mild To Severe Alzheimer's Disease Residing In An Assisted Living Facility

This is a study to determine the effectiveness and safety of donepezil hydrochloride (E2020) used to treat residents of assisted living facilities diagnosed with mild, moderate, or severe stage Alzheimer's disease.

Birmingham, Alabama, United States+35 moreView details
CompletedPhase 1

Safety and Tolerability of Dimebon in Patients on Memantine, and Memantine Plus Donepezil

The purpose of this study is to evaluate the safety and tolerability of dimebon given to Alzheimer's disease patients currently on a stable dose and regimen of memantine or memantine plus donepezil.

Los Alamitos, California, United States+3 moreView details
CompletedPhase 1 / Phase 2

Specialized Food Plan Based on Individual Physiological Comprehensive Body Assessments Accompanied With Cellular Repair Therapy to Decrease Inflammation Cognitively Impaired Patients

Diet plays a large role in inflammation, oxidative stress and cognition; however, every person's body type, resting metabolic rate, BMI, and inflammation levels vary. Through performing physiological and comprehensive cellular testing throu

Scottsdale, Arizona, United StatesView details
Completed

Blood Biomarker of Alzheimer's Disease (AD)

Currently, no cures or disease modifying therapies exist for Alzheimer's disease (AD). This is partially due to the inability to detect the disease before it has progressed to a stage where there are clinical manifestations.

Durham, North Carolina, United StatesView details
CompletedN/A

Effects of Strength Exercise on Fall Risk in Elderly With Alzheimer's Disease

Interventional study to show the effects of strength exercise on fall risk in elderly with Alzheimer's disease

Jaén, Andalusia, Spain+1 moreView details
RecruitingN/A

Testing & Refinement of CarePair: An Assessment and Referral Platform to Support Family Caregivers of Alzheimer's Disease and Related Dementias.

The purpose of this study is to develop and test CarePair, a mobile application-based needs assessment and service referral platform for family caregivers of persons with dementia designed to alleviate stress and promote psychosocial well b

Los Angeles, California, United StatesView details
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